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Alzheimer’s Disease Polygenic Scores Predict Changes in Episodic Memory and Executive Function Across 12 Years in Late Middle Age

Authors :
Daniel E. Gustavson
Chandra A. Reynolds
Timothy J. Hohman
Angela L. Jefferson
Jeremy A. Elman
Matthew S. Panizzon
Michael C. Neale
Mark W. Logue
Michael J. Lyons
Carol E. Franz
William S. Kremen
Source :
J Int Neuropsychol Soc, Journal of the International Neuropsychological Society : JINS, vol 29, iss 2
Publication Year :
2022
Publisher :
Cambridge University Press (CUP), 2022.

Abstract

Objective:Alzheimer’s disease (AD) is highly heritable, and AD polygenic risk scores (AD-PRSs) have been derived from genome-wide association studies. However, the nature of genetic influences very early in the disease process is still not well known. Here we tested the hypothesis that an AD-PRSs would be associated with changes in episodic memory and executive function across late midlife in men who were cognitively unimpaired at their baseline midlife assessment..Method:We examined 1168 men in the Vietnam Era Twin Study of Aging (VETSA) who were cognitively normal (CN) at their first of up to three assessments across 12 years (mean ages 56, 62, and 68). Latent growth models of episodic memory and executive function were based on 6–7 tests/subtests. AD-PRSs were based on Kunkle et al. (Nature Genetics, 51, 414–430, 2019), p −8 threshold.Results:AD-PRSs were correlated with linear slopes of change for both cognitive abilities. Men with higher AD-PRSs had steeper declines in both memory (r = −.19, 95% CI [−.35, −.03]) and executive functioning (r = −.27, 95% CI [−.49, −.05]). Associations appeared driven by a combination of APOE and non-APOE genetic influences.Conclusions:Memory is most characteristically impaired in AD, but executive functions are one of the first cognitive abilities to decline in midlife in normal aging. This study is among the first to demonstrate that this early decline also relates to AD genetic influences, even in men CN at baseline.

Details

ISSN :
14697661 and 13556177
Volume :
29
Database :
OpenAIRE
Journal :
Journal of the International Neuropsychological Society
Accession number :
edsair.doi.dedup.....822344565f2c785e84b3f6fc54d91bd2
Full Text :
https://doi.org/10.1017/s1355617722000108